Herbicidal organophosphorus-nitrogen compositions and method using same



United States Patent Office 3,511,632 Patented May 12, 1970 3,511,632 HERBICIDAL ORGANOPHOSPHORUS-NITROGEN COMPOSITIONS AND METHOD USING SAME John C. Wollensak, Royal Oak, Kenneth M. 'Chn'stenson, Detroit, and David W. Zutaut, Pleasant Ridge, Mich., assignors to Ethyl Corporation, New York, N.Y., a corporation of Virginia No Drawing. Filed Aug. 4, 1967, Ser. No. 658,321 Int. Cl. AOln 9/36 US. C]. 7186 2 Claims ABSTRACT OF THE DISCLOSURE Formulations containing organophosphorus-nitrogen compounds are useful plant defoliants and herbicides.

The active compounds in such formulations have the general formula:

ii/ R NR P wherein R and R are alkyl, alkenyl, aryl, aralkyl, alkaryl, and alicyclic groups having up to 12 carbon atoms; R is hydrogen or a hydrocarbon group as described for R and R and X is oxygen or sulfur.

Background of the invention This invention relates to the control of undesirable vegetation in general. More specifically, it pertains to the partial or total modification of the growth of plants, including defoliation and the complete suppression or eradication of plants. Many of the compounds employed in this invention and a process for their preparation have been reported in the literature; Michaelis, Chem. Ber. 31, 1037 (1898).

Summary of the invention The instant invention is directed to controlling undesirable vegetation by a method which comprises contacting the vegetation with a herbitoxic amount of an organophosphorus-nitrogen compound. The herbitoxic compositions of this invention may be in the form of a solution, an emulsifiable oil, a wettable powder, dust, granules, or aerosol. Depending on the specific type of the formulation, there may additionally be present a surfactant, a carrier, or an adjuvant.

Description of the preferred embodiments The novel herbitoxic compositions of this invention contain as an active ingredient an organophosphorus nitrogen compound having the formula:

wherein R and R which may be the same or different, are hydrocarbon groups having up to about 12 carbon atoms, or hydrocarbon groups containing various substituents thereon, and being selected from the group consisting of alkyl, alkenyl, aryl, alkaryl, aralkyl and alicyclic groups; R is hydrogen or an unsubstituted or a substituted hydrocarbon group containing up to about 12 carbon atoms, and being selected from the group con sisting of alkyl, alkenyl, aryl, aralkyl, alkaryl and alicyclic groups; and X is oxygen, sulfur or selenium.

Examples of alkyl groups which may be present in the above general formula are methyl, ethyl, propyl, iso propyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-amyl, and the various positional isomers thereof as, for example, l-methylbutyl, Z-methylbutyl, S-methylbutyl, 1,1- dimethylpropyl, and the like, and likewise the corresponding straightand branched-chain isomers of hexyl, heptyl, octyl, nonyl, decyl, undecyl, and dodecyl.

Examples of alkenyl groups that may be employed in the compounds of this invention are ethenyl, l-propenyl, 2-propenyl, isopropenyl, l-butenyl, 2-butenyl, S-butenyl, and the corresponding branched-chain isomers thereof such as l-isobutenyl, 2-isobutenyl, l-sec-butenyl, 2-secbutenyl, including l-methylene-Z-propenyl, l-pentenyl, Z-pentenyl, 3-pentenyl, 4-pentenyl, and the corresponding branched-chain isomers thereof as well as all isomers of hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, and dodecenyl as, for example, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, l-methyl-l-ethyl-2-propenyl, and the like.

Examples of aryl groups which may be present in the above formula are phenyl and naphthyl groups. Alkaryl groups which may also be present are tolyl, 2,3-xylyl, 2,4-xylyl, 2,5-xylyl, 2,6-xylyl, 3,4-xylyl, 3,5-xy1yl, o, m, and p-cumenyls, mesityl, o, m, and p-ethylphenyl, 2- methylnaphthyl, 3-methylnaphthyl, 4-methylnaphthyl, 5- methylnaphthyl, 6-methylnaphthyl, 7-methylnaphthyl, 8- methylnaphthyl, l-ethylnaphthyl, the various positional isomers of these naphthyl radicals, and the like. Some of the examples of aralkyl groups are benzyl, phenylethyl, a-phenylpropyl, B-phenylpropyl, oz and p-phenylisopropyl radicals, on and fl-phenylbutyl radicals, and the like.

Alicyclic groups which may be present in the above formula are exemplified by cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, and the like, or alkyl derivatives of said alicyclic groups such as a-cyclobutylpropyl, ,B-cyclobutylpropyl, and similar higher derivatives.

In the preferred class of compounds, R is an alicyclic group, R is hydrogen, and R is an alkyl group having up to 12 carbon atoms. The most preferred compound is di-n-butyl cyclohexylphosphoramidate.

Illustrative but non-limiting examples of typical active ingredients of this invention are listed below.

(1) S,S,-bis(2-bromo-n-butyl) (hexahydro-p-tolyl) phosphoramidothioate (2) Bis (p-hydroxyphenyl cyclobutylphosphoramidotrithioate (3 Dicyclohexyl 3 -chlorocyclohexyl) phosphoramidate (4) Diethyl [4- (4-tert-butyl-2,6-diethylphenyl) -nbutyl] phosphoramidate (5 Dioctadecyl ethyloctadecylphosphoramid ate (6) Bis(2,5-dichlorophenyl) (p-nitropheny1)-3,5-

xylylphosphoramidate (7) 0,0-diallyl-n-undecylphosphoramidothiate (8 QO-dicyclopentyl (4-nitro-n-hexyl phenylphosphoramidoselenoate (9) 0,0-bis (p-nitrophenyl) (6-amino-n-hexyl) (2- bromo-n-propyl)phosphoramidoselenoate 10) Bis(S-cyano-n-pentyl)-3-pentenylphosphoramidate (1 1 Bis(Z-hydroxyethyl) (l-chloroethyl) cyclohexylphosphoramidate (12) 0,0-diallyl(3-fiuoro-p-tolyl)phosphoramidothiate (13) Bis( p-aminophenyl) p-aminophenyl )phosphoramidotrithioate 14) Diethyl( 1,2-dihydroxyethyl phosphoramidate (15) 0,0-bis pentachloroethyl bis( 2,5 -diodobenzyl) phosphoramidothiate The above groups which may be present in the general formula may contain various substituents such as halogens, hydroxy, amino, nitro, and the like. Illustrative examples of groups having such substituents are chloromethyl, 2-bromobutyl, 1-iodo-2-propenyl, chlorophenyl, 4-chlorotolyl, 1-phenyl-2-chloropropyl, fiuorocyclohexyl,

3-hydroxypropyl, l-hydroxy-3-pentenyl, hydroxyphenyl, Z-hydroxytolyl, l-phenyl-3-hydroxypentyl, hydroxycyclopentyl, Z-nitrobutyl, nitrophenyl, Z-nitrotolyl, l-phenyl-4- nitrohexyl, nit-rocyclobutyl, Z-aminobutyl, Z-aminobutenyl-l, aminophenyl, 2-nitro-4-aminophenyl, 2-chloro-3- nitrophenyl, l-hydroxy-B-bromohexyl, and the like.

The class of compounds represented by the general formula on page 1 may be prepared by various methods available in the art. For the purpose of this invention, it is immaterial what specific method of preparation is employed since our invention is primarily concerned with the unobvious use of said class of compounds as herbitoxic materials. One method of preparation of the compounds of this invention is reported by Michaelis, Chem. Ber. 31, 1037 (1898).

In a preferred embodiment, the compositions of this invention contain an active ingredient (a compound of the type formulated and enumerated above and exem plified below) and a surfactant as a dispersant thereof. In a more preferred embodiment, the herbitoxic compositions contain an inert carrier as well as a surfactant and active ingredient. Typical surfactants and carriers employed in this invention are discussed below.

The methods provided by this invention for treating undesirable vegetation comprise contacting living plant tissue with one or more of the active ingredients described and enumerated above and exemplified below. In a more preferred embodiment, undesirable vegetation is treated with a composition comprising one or more active ingredient, a surfactant as a dispersant therefor, and an inert carrier.

The surfactants or conditioning agents employed in the instant invention extend the active ingredient and promote its intimate contact with the vegetation to which it is applied. They also aid in the adaptation of the active ingredients for use in conventional application equipment. In general, from 0.1 to percent by weight of a surfactant is employed in the compositions of this invention; however, greater and smaller amounts can be used, if desired.

Typical examples of surfactants which are suitable for use in this invention are soaps, saponins, gelatin, casein, flour, sulfite lye, synthetic cationic, anionic, and nonionic surfactants, and the like. Detailed lists of such agents are set forth by J. W. McCutcheon in Soap and Chemical Specialities, December, 1957; January, February, March, and April, 1958; and in Detergent and Emulsifiers Up to Date-4960, John W. McCutcheon, Inc., 475 Fifth Avenue, New York, NY. A further discussion of surface active wetting agents is set forth by D. E. H. Frear in Chemistry of Insecticides, Fungicides and Herbicides, 277-287, published by D. Van Nostrand Company, Inc. (1948).

The materials commonly known as carriers comprise another type or ingredient which is preferably employed in the compositions of this invention. The purpose of a carrier is to extend and facilitate the application of the active ingredient to the vegetation upon which it is applied. In general, carriers may be of two types; viz., solids and liquids. Liquid carriers include well-known liquids such as water and various organic formulations. Typical liquid organic carriers are petroleum fractions such as kerosene and diesel fuel, aromatics such as benzene and toluene, ketones such as acetone and methylethylketone, esters such as amyl acetate, octyl acetate, and the like.

Typical solid carriers are inert solid extenders of mineral origin such as Fullers earth, kaolin, bentonite, china clay, various magnesium silicates, gypsum, pumice, mica, talc, attapulgite clay, and the like. Inert extenders of vegetable origin, such as soy bean flour, tobacco flour, ground walnut shells, ground pecan shells, and the like can also be employed.

The herbicidal compositions of the present invention can also beneficially contain other adjuvants. Examples of such further adjuvants are corrosion inhibitors, perfumes, dyes, odor-masking agents and stabilizers. In addition, other herbicidal, fungicidal, or insecticidal agents might be mixed with the herbicidal compositions of ths invention in order to obtain enhanced or dual effects from the application of the resultant composition.

One formulation for applying the active compounds of this invention to undesirable plants is a solution or suspension of the active compound in a suitable aqueous or organic medium. The organic medium may be a volatile solvent or it may be a higher boiling solvent such as kerosene.

When using a solution or suspension formulation, a preferred active ingredient concentration range is from about 0.5 to 100 parts by weight active igredient per 250 parts by weight of formulation, although more or less can be used. A more preferred concentration range is from about 1 to 50 parts by weight active ingredient per 250 parts of formulation. A most preferred concentration range is from about 1 to 10' parts by weight active ingredient per 250 parts of formulation.

Emulsifiable oil formulations which are solutions or suspensions of the active compound in water-immiscible solvents together with a surface active agent may also be used. In these formulations the water-immiscible solvent is the carrier. Suitable waterimmiscible solvents for the active compound of this invention are hydrocarbons, such as k rosene, or xylene, and water-insoluble ethers such as dibutyl Carbitol and dibutyl Cellosolve, esters such as as amyl acetate and octyl acetate, and ketones such as methyl ethyl ketone or dioctyl ketone. The solvent concentration may be from 10 to 50 to about 70 weight percent. The surfactant may be employed in a concentration from 0.5 to about 15 weight percent.

A preferred active ingredient concentration of the emulsifiable oil formulations of the present invention is from about 10 to about 90 weight percent. A more preferred active ingredient concentration in these formulations is from about 20 to about weight percent. A most preferred active ingredient concentration in the emulsifiable oil formulations of this invention is from about 25 to about 50 weight percent.

The compositions of this invention may be formulated in the form of wettable powders. These are water dispersible compositions which contain, in addition to the active compound, an inert solid extender and one or more surfactants which perform the functions previously set out. The preferred inert solid extenders used in this invention are of mineral origin, such as Fulle-rs earth, kaolin, bentonite, china clay, and the like.

A preferred active ingredient concentration of the wettable powder formulations of this invention is from about 10 to about 90 weight percent. A more preferred active ingredient concentration is from about 20 to about weight percent, and a most preferred active ingredient concentration in the wettable powder formulations of this invention is from about 50 to about 80 weight percent. The surfactant concentration may be from 0.5 to about 15 weight percent and preferably from 1 to about 5 weight percent. An inert carrier may be used in the amount from 10 to weight percent and more preferably from 10 to 50 weight percent.

Dusts are powder formulations which are intended for application in the dry form. The dust should be free flowing and have a high density. Dust formulations can contain the active compounds, an inert extender, a surfactant, and may also contain a wetting agent and a grinding aid.

A preferred active ingredient concentration employed in the dust compositions of this invention is from about 0.1 to about 25 weight percent, and more preferably, from about 1 to about 10 weight percent. The surfactant concentration may be from about 0.01 to about 5 weight percent, and more preferably, from about 0.5 to about 1 weight percent. The balance of the dust compositions of this invention comprise inert free flowing dust and any other adjuvants that might be desired, such as corrosion inhibitors, anti-foam agents, dyes, and the like.

Granule formulations may also be employed. Granules are compositions of macroscopic dimension containing the active ingredient, generally a surface active agent, and a carrier. Suitable carriers for granule formulations are clays, pyrophyllite and vermiculite.

A preferred active ingredient concentration of the granular formulations of this invention is from about 1 to about 50 weight percent, and more preferably, from about to about 30 weight percent. A preferred surfactant concentration employed in the granular formulations is from about 0.01 to about weight percent, and a more preferred is from about 0.1 to about 1 weight percent. The balance of the granular formulations is preferably made up of about to 30 mesh particulate inert mineral carrier.

The compounds of this invention are also effective when formulated in aerosol formulations. In these formulations, the active compounds are dissolved in an extremely volatile solvent known in the art for this purpose and maintained under pressure in a confined space.

The active ingredients described in this invention are also useful in colloidal formulations. A colloidal formulation is prepared by passing a mixture of the active ingredient, a hydrocarbon solvent, and a large amount of water through a colloid mill until homogenation of the oil and water is achieved.

The above-discussed formulations and additives are disclosed in greater detail in a copending application Ser. No. 530,778, filed Mar. 1, 1966, now US. Pat. 3,409,- 424.

The compounds used in the following Examples 1 to 7 will have the designations given below:

(A) Di-n-butyl cyclohexylphosphoramidate (B) Bis (Z-methyl-n-butyl) phenylphosphoramidate (C) 0,0-diphenyl(p-hydroxyphenyl)phosphoramidothioate (D) 0,0-bis(p-aminophenyl) (2-chloro-n-propyl) phosphoramidothioate (E) Dicyclohexyl(S-Cyano-n-propyl)phosphoramidate (F) S,S-bis(p-nitrophenyl)methylphosphorarnidoselenodithioate (G) 0,0-dioctadecyl (hexahydrobenzyl) phosphoramidothioate (H) Bis(2-chloro-n-butyl) (6-cyano-n-hexyl) (4- hydroxy-n-butyl)phosphoramidate The following examples serve to illustrate the herbitoxic formulations of this invention. All percentages are by weight.

EXAMPLE 1 Percent Compound A 50 Bentonite 49 Sodium alkyl benzene sulfonate 1 EXAMPLE 2 Percent Compound B 90 Sodium alkyl naphthalene sulfonate -o 0.5 Kaolin I 9.5

The above wettable powder is prepared in the same manner as in Example 1. For application, it is dispersed in water at a rate equivalent to 10- pounds of active ingredient per 30 gallons of water.

In the above example, similar formulations are prepared containing 20, 30, 40, 50, 60, 70, 80, or 90 percent Compound C and correspondingly smaller amounts of carrier.

EXAMPLE 3 Percent Compound D 10 Talc Diatomaceous silica 8 Fatty acid amides 2 The above dust is prepared by first grinding together the active ingredients, diatomaceous silica and fatty acid amide and then blending in the talc and thoroughly mixing.

This dust formulation can be applied using a tractor or airplane-mounted duster, at a rate of about 5 pounds of active ingredient per acre.

EXAMPLE 4 Percent Compound E 25 Diesel fuel 65 Alkylaryl polyether alcohols 10 EXAMPLE 5 Percent Compound F 30 Sodium alkyl naphthalene sulfonate 5 1530 mesh attapulgite 65 The above granular composition is prepared by first dissolving the active ingredient and surface active agent in water and then spraying the solution on the carrier. Following this, the granules are dried. It may then be applied to plant tissue at a rate of from about 1 to 10 pounds of active ingredient per acre.

In the above example, similar formulations are prepared containing 10, 40, 60, 80, and percent of Compounds E and F, and correspondingly smaller amounts of the attapulgite.

EXAMPLE 6 Into a cylinder rated at p.s.i.g. working pressure is introduced 10 parts of Compound G. The cylinder is then made pressure tight except for one opening, through which is introduced a mixture of 10 parts of acetone and 50 parts of dichlorodifluoromethane, from a container holding this material under 2000 p.s.i.g. The cylinder into which the ingredients have been introduced is then sealed off and shaken to give a uniform solution ofv the active compound in the volatile solvents. When sprayed into the atmosphere this solution Will form an effective aerosol of the active compound employed.

In the above example, similar formulations are prepared containing 10, 30, 60 and 90 percent of Compound G and correspondingly smaller amounts of the solvent.

EXAMPLE 7 A colloidal formulation is prepared by passing a mixture of 10 parts of Compound H, 100 parts of kerosene, 1000 parts of water, and 1 part of mannitan monooleate through the colloid mill until homogenation of the oil in water is achieved.

EXAMPLES 8 to 112 Compounds 115 set forth above are incorporated, one

7 at a time, in each of the foregoing Examples 1 through 7.

The compositions of this invention are extremely useful when employed in the method of this invention for controlling the growth of undesirable vegetation. Not only are they phytotoxic to many undesirable plants, but they are also useful as defoliants. The compositions of this invention are active as plant growth regulants at rates as low as one-tenth pound of active ingredient per acre. A preferred application rate is from 1 to 60 pounds of active ingredient per acre, and a most preferred application rate is from 5 to pounds of active ingredient per acre. Higher or lower rates can be employed, depending upon the effect that the particular user desires to accomplish.

The compositions of the present invention are usually contacted with the leaves and stems of growing plants in the terms broadest sense, but can be applied to soil to obtain pre-emergence herbitoxic effects.

As appreciated in the art, the morphological effect obtained with the active ingredients of this invention may be influenced by the application rate, ambient temperature, humidity, and the time of the life cycle of the plant to which the compositions are applied. The effect usually desired of plant growth regulators is either defoliation or complete eradication of undesirable species. It is in these particular applications that the compositions of this invention are most useful. The following tests were carried out in order to demonstrate the useful properties of the compositions of this invention.

In test procedure A, the compounds were formulated as follows. Each compound was weighed into a small aluminum cup. The material was then washed into small beakers with about 5 ml. of acetone, followed by ml. of water, giving a total volume of ml. A quantity of this material containing 31 mg. of the test compound was then removed and water added to it to bring its volume to 11 ml. At this point, 0.5 ml. of a one weight percent solution of Triton X-155 was added to the test solution and its volume then raised to 15 ml. by the addition of water. When this test solution is sprayed over an area of onethird square yard, it approximates an application rate of 30 gallons per acre containing one pound of test chemical per acre.

In some experiments the test compound was merely dissolved in acetone, so that 12 ml. of acetone solution contained 31 mg. of test compound.

The spray chamber used in carrying out subsequent tests was about 36 inches wide, 18 inches deep, and 26 inches high. It was made of clear plastic and the front of the chamber had sliding doors suitable for placing,

plants in and removing plants from the chamber. The top of the chamber had a hole for introducing the spray.

The compounds were examined by spraying them on l4-day-old Black Valentine bean plants and in some instances on privet plants at a rate equivalent to one pound of test compound per acre.

In the following Table I, the effectiveness of the compounds of this invention are expressed in terms of their phytotoxicity and their ability to cause abscission (defoliation). The abscission value is expressed in terms of the percentage drop of the total leaves on the plant (percent defoliation). At the time of spraying, the bean plants usually have two primary leaves. However, during the 14 days the plant is observed following spraying, two more (trifoliate) leaves usually emerge. Dropping of the two primary leaves would be recorded as 50 percent abscission. Dropping of all four leaves would be recorded as 100 percent abscission. Actually, dropping of the two primary leaves would constitute a total drop of all leaves actually contacted with the test compound.

Phytotoxicity is a measure of leaf damage (not to be confused with leaf droppage) and is estimated visually on a scale from 0 to 11, where 0 indicates no effect and 11 indicates all leaves killed. It is possible for a test chemical to have a phytotoxicity rating of 11 and yet have an {.Abcission and phytotoxicity ratin s of di-n-butyl cyclohexylphosphoramidate on black valentine beans] Percent Concentration defoliation Phytotoxicity 0.1 lb./acre (Wat-er) 0 2 1.0 lb./acre (water) 0 1.01b./acr e (acetone). 75 1 Further tests were carried out to demonstrate the selectivity of the compositions of this invention. Test procedure B consisted of formulating the test compound in either water or acetone mixtures as previously described. The formulated test compounds were then sprayed on American Elm, Pin Oak, Euonymus, and Boxwood. Observations were made at specific intervals, such as at the end of 3, 8 and 13 days. The extent of abscission (defoliation) was rated as either light (-L), moderate (M), severe (S), or total (T). The phytotoxicity was rated on the same scale (0 to 11) as was used in the Black Valentine bean tests. Table II shows the results obtained when din-butyl cyclohexylphosphoramidate was used at rates equivalent to 1 and 5 pounds per acre.

TABLE II [Abscission and phytotoxicity ratings of di-n-butyl cyclolie-xylphosphoramidate on deciduous and evergreen trees] Abscission Phytotoxicity 5 lbI/acre (water) 5 lbJacre (acetone)- 1 Hoe 000 Hfc E ub: HHO mml- Still further tests were carried out on the compounds of this invention to more fully determine the effectiveness of such compounds. In test procedure C, the test compound was dissolved in acetone containing 0.5% Tween-20. The concentrations were adjusted so that rates of 1.0 lb.-/acre and 0.1 lb./acre could be applied. Each rate was applied in duplicate to six different 7- day old species. The test plants used were Black Valentine bean, Heavenly Blue Morning-Glory, Scarlet Globe Radish, Lincolon Soybean, Clinton Oats and Rice (P1. 8970). At selected time intervals, the following effects were noted: abscission, chlorosis, contact injury, curvature, formative effects, galling, killing, necrosis, abnoraml pigmentation, quilling, adventitious roots, and stunting. A rating system ranging from a value of l to 4 was used for each species. When the plant appeared normal, a rating of one was assigned, whereas when the plant was killed, a value of 4 was assigned. Thus, the ratings are such that a maximum value of 4 for each species may be obtained. Since there are six species and each may obtain a value of from one to four, the overall result will always fall within the range of from 6- to 24. The latter indicates complete kill of all the species. The former indicates no eifect. Final readings are obtained 10 to 14 days after application. The following Table III shows the final overall result obtained when the indicated organophosphorus compounds were applied on the above-described six species.

TABLE III [Summary hervicidal properties of di-n-butyl cyclohcxylphosphoramidate] Rating (based on a Concentration maximum value of 24) 0.1 lb./acre 6 1.01b./acre 16 In test procedure D, the test compounds dissolved 10 in acetone containing 0.5% Tween-20 were sprayed at 10, 5 and 1 pound per acre concentrations, usually on eight species: Hemlock, Spruce, Elm, Locust, Oak, Privet, Pine, and Maple. After about two weeks, the results of the test were noted and expressed as no effect slight (S), moderate (M), or extreme (E) abscission and contact effect (desiccation), and kill, as shown in Table IV below.

TABLE IV [Abscission and contact ratings of di-n-butyl cyclohexylphosphoramidate] Concentrations 1 lbJacre 5 lbJacre 10 lb./acre Hemlock:

Abscission Contact S S Spruce:

Abseission S Contact S S lm:

Abscissiom S Contact S M Locust:

Abscission ontact Abscission Contact Privet:

Abscissiom Contact e:

Abscissiom Contact Maple:

Abscission S Contact S S M As noted above, certain herbitoxic formulations require an organic medium or a solvent. In addition to the solvents and the organic medium materials listed above, alcohols and sulfoxides may also be employed. Nonlimiting examples of alcohols are l-butanol, cyclohexanol, l-octanol, l-nonanol, and the remaining positional isomers, Z-methyl-l-nonanol, 2,8-dimethyl-5-nonanol, l-dodecanol, 6-dodecanol, l-tetradecanol, all positioned isomers thereof, and the like. Illustrative examples of sulfoxides are dimethyl sulfoxide, diethyl sulfoxide, di-npropyl sulfoxide, di-n-butyl sulfoxide, dibenzyl sulfoxide, and the like.

This invention can be extended to the treatment of species of plants other than those mentioned above, such as algae.

Having fully described the compositions of this invention and their novel uses, it is desired that this invention be limited only within the lawful scope of the appended claims.

What is claimed is:

1. A method of controlling undesirable vegetation, said method comprising contacting said vegetation with a herbicidal amount of a compound having the formula:

wherein R and R are hydrocarbon radicals independently selected from the group consisting of alkyl and alicyclic groups having up to about 12 carbon atoms, X is selected from the group consisting of oxygen and sulfur.

2. The method of claim 1 wherein said compound is di-n-butyl-cyclohexylphosphoramidate.

References Cited UNITED STATES PATENTS 2,929,762 3/1960 Wasco et a1. 7l86 X JAMES O. THOMAS, 1a., Primary Examiner US. Cl. X.R. 

